Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-(4-[1,2,3]Triazol-1-yl-butyl)phenol | HCID 12109494 | — |
| Reactant | 4-(Chloromethyl)-2-{2-[4-(difluoromethoxy)phenyl]ethenyl}-1,3-oxazole | HCID 69112574 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69475972 | HCID 69475972 | — |
Reaction Steps
0.286 g (1.00 mmol) 4-Chloromethyl-2-[2-(4-difluoromethoxy-phenyl)-vinyl]-oxazole, 0.217 g 1.00 mmol) 4-(4-[1,2,3]Triazol-1-yl-butyl)-phenol, 0.166 g (1.00 mmol) potassium iodide and 0.191 ml (1.00 mmol) of a 30% sodium methylate solution were added to 50.0 ml methanol and heated to reflux for 12 h. After removal of solvent, partitioning of the residue between 50 ml ethyl acetate and 15 ml water, the organic phase was washed with 10 ml water, 10 ml 0.1 N NaOH, 15 ml water twice and dried over sodium sulphate. The solution was concentrated to a volume of 5 ml until crystallisation of the product started. After leaving for 1 h at room temperature the precipitate was sucked off, washed with ether and dried at 40° C. in vacuo. Yield 0.20 g (43%) 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205325B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-b3c6824d816646d686b72dce51dc135b |
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| Source note | uspto-grants-2007_04 |
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